Resources & Insights

For years, pharmaceutical and biotechnology companies have employed the strategy of establishing preferred provider relationships in order to streamline the process of outsourcing clinical research studies. Often, the preferred provider would provide discounts to their customers based on efficiencies the service provider may realize from working on multiple trials for a single compound or the…

RESEARCH TRIANGLE PARK, N.C. (June 1, 2016) — PharPoint Research, a U.S.-based contract research organization (CRO), today announced the expansion of their clinical trial management and consulting service capabilities into Europe. The extension provides PharPoint Research’s global drug development clients greater access to increasingly meaningful markets and increases their reach across the European continent. With rising…

PharPoint Research, Inc., a drug development service company providing biostatistics and data management services to the pharmaceutical and biotechnology industries, announces that it has incorporated Medrio’s EDC technology platform into its growing suite of data management applications. “The addition of Medrio’s EDC solution to our existing offerings further supports PharPoint’s ability to consistently exceed our…

Medidata Solutions (NASDAQ: MDSO), a leading global provider of SaaS-based clinical development solutions, announced that PharPoint Research, Inc., a North Carolina-based drug development service company, has joined Medidata’s ASPire to Win® channel partner program, bringing the program’s partner count to 30 organizations. With this partnership, PharPoint will be able to offer the Medidata Rave® electronic data capture (EDC) and clinical data…

Adaptive Trial Design and the Shifting CRO Landscape This article was originally published on the Medrio blog on May 7, 2019, discussing outsourcing, adaptive trial design, and more. You can view the original post here. Anyone with more than a few years’ experience in the clinical research industry has been witness to major industry shifts,…

As an old clinical technology geek, I have  always been interested in new advances in the collection of clinical trial data. Since my initial position in the industry in 1989, I have seen a lot of clinical data collection ideas come and go.  I remember working with Remote Data Entry (RDE) in the early 90’s,…

Patient recruitment used to be an ad hoc affair, where sites were personally selected by a sponsor and given a few hundred dollars to create local awareness for a clinical trial. The sponsor’s hope was that the investigator grants would be competitive enough to keep sites motivated, but unsurprisingly this approach resulted in numerous trials…

At PharPoint, we pride ourselves on producing quality statistical analyses. How are we so confident in the quality of our product? Find out in this video with Senior Manager of Statistical Programming Tracy Pflaumer and Manager of Statistical Programming Amber Urban.